N-Acetyl-DL-methionine

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Names

[ CAS No. ]:
1509-92-8

[ Name ]:
N-Acetyl-DL-methionine

[Synonym ]:
Methionine, N-acetyl-, DL-
(R)-N-acetylmethionine
2-(acetylamino)-4-(methylthio)butanoic acid
MFCD00069962
D-Methionine, N-acetyl-
N-acetyl-methionine
DL-Methionine, N-acetyl-
N-Acetyl-D-methionine
Methionine, N-acetyl-
N-ACETYLMETHIONINE, D-
ACETYL-DL-METHIONINE
N-Acetylmethionine
UNII:383941IGXN
EINECS 216-144-4
N-α-Acetyl-D-methionine
Ac-DL-Met-OH
DL-N-Acetylmethionine
(2R)-N-acetylmethionine

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
453.6±40.0 °C at 760 mmHg

[ Melting Point ]:
117-119ºC

[ Molecular Formula ]:
C7H13NO3S

[ Molecular Weight ]:
191.248

[ Flash Point ]:
228.1±27.3 °C

[ Exact Mass ]:
191.061615

[ PSA ]:
91.70000

[ LogP ]:
-0.19

[ Vapour Pressure ]:
0.0±2.4 mmHg at 25°C

[ Index of Refraction ]:
1.511

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Acetamide
  • Methional
  • carbon monoxide
  • N-acetyl-DL-homocysteine
  • N-Acetyl-DL-methionine
  • Methyl methioninate
  • L-Methionine, methylester(H-Met-OMe)
  • D-methionine
  • Ethanoic anhydride

DownStream

  • D-methionine

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Importance of product inhibition in the kinetics of the acylase hydrolysis reaction by differential stopped flow microcalorimetry.

Anal. Biochem. 308 , 285-293, (2002)

The hydrolysis of N-acetyl-L-methionine, N-acetylglycine, N-acetyl-L-phenylalanine, and N-acetyl-L-alanine at 298.35K by porcine kidney acylase I (EC 3.5.1.14) was monitored by the heat released upon ...

Model sclerotization studies. 4. Generation of N-acetylmethionyl catechol adducts during tyrosinase-catalyzed oxidation of catechols in the presence of N-acetylmethionine.

Arch. Insect Biochem. Physiol. 38(1) , 44-52, (1998)

Incubation of catechol with mushroom tyrosinase in the presence of N-acetylmethionine resulted in the generation of an adduct. This product was identified to be N-acetylmethionyl catechol, on the basi...

Identification of N-acetylmethionine as the product released during the NH2-terminal processing of a pseudo-class I actin.

J. Biol. Chem. 264(19) , 11491-6, (1989)

Genes for the various isoactins define two classes of actin. Class I actin genes code for Met-Asp(Glu)-actin, and class II actin genes code for Met-X-Asp(Glu)-actin where X is usually cysteine. Amino ...


More Articles

Related Compounds

  • N-Acetyl-DL-methionine
  • N-Acetyl-DL-methionine
  • N-acetyl-dl-methionine magnesium
  • Allantoin N-acetyl-DL-methionine
  • N-ACETYL-DL-MET NH2
  • N-Acetyl-DL-serine methyl ester
  • 3-[(4-Methylpentan-2-yl)oxy]azetidine
  • 2-Amino-7-iodo-3-methylquinazolin-4(3H)-one
  • 7-Hydroxy-3-methyl-2-phenyl-6-quinoxalinecarboxylic acid
  • 3-(2,3-Dimethoxyphenyl)-2-methylpropan-1-amine
  • 2-(3,5,6-Trifluoropyridin-2-yl)propan-1-ol
  • 2-(Tert-butoxycarbonylamino)pyrazolo[1,5-a]pyridine-3-carboxylic acid
  • Tert-butyl 2-(3-amino-4-cyanophenyl)acetate
  • Tert-butyl 2-amino-2-(4-chlorophenyl)butanoate
  • (2R)-2,6,6-Trimethylheptanoic acid
  • (2S)-3-Cycloheptyl-2-methylpropanoic acid
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